Genetic Variations Strongly Influence Phenotypic Outcome in the Mouse Retina (Q30474767)

19 October 2017

Genetic variations strongly influence phenotypic outcome in the mouse retina (English)

1 reference

19 October 2017

Genetic Variations Strongly Influence Phenotypic Outcome in the Mouse Retina (English)

1 reference

10.1371/JOURNAL.PONE.0021858

DOI

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0021858

7 December 2024

author name string

Yang Yuan

2

1 reference

19 October 2017

Fang Qiu

6

1 reference

19 October 2017

Sarah Schenk

7

1 reference

19 October 2017

Austin S. Jelcick

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21779340

7 December 2024

Barrett D. Leehy

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21779340

7 December 2024

Lakeisha C. Cox

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21779340

7 December 2024

Alexandra C. Silveira

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21779340

7 December 2024

Andrew J. Sachs

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21779340

7 December 2024

Margaux A. Morrison

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21779340

7 December 2024

Arne M. Nystuen

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21779340

7 December 2024

Margaret M. DeAngelis

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21779340

7 December 2024

Neena B. Haider

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21779340

7 December 2024

language of work or name

English

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publication date

14 July 2011

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full work available at URL

19 October 2017

https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0021858&type=printable

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open access

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21779340

https://europepmc.org/articles/PMC3136482

7 December 2024

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21779340

https://europepmc.org/articles/PMC3136482?pdf=render

7 December 2024

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open access

content deliverer

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:21779340

http://dx.plos.org/10.1371/journal.pone.0021858

7 December 2024

1 reference

10.1371/JOURNAL.PONE.0021858

DOI

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0021858

7 December 2024

1 reference

19 October 2017

6

1 reference

19 October 2017

7

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19 October 2017

e21858

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Creative Commons Attribution 4.0 International

19 October 2017

start time

14 July 2011

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April 2022 Public Data File from Crossref

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Genetic modifiers of retinal degeneration in the rd3 mouse

20 June 2018

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Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene

20 June 2018

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Genetic modification of the schisis phenotype in a mouse model of X-linked retinoschisis

20 June 2018

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The polymorphism architecture of mouse genetic resources elucidated using genome-wide resequencing data: implications for QTL discovery and systems genetics

20 June 2018

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A typology of photoreceptor gene expression patterns in the mouse

20 June 2018

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20 June 2018

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20 June 2018

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A high-resolution map of segmental DNA copy number variation in the mouse genome

20 June 2018

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Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration

20 June 2018

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The Notch ligand JAG1 is required for sensory progenitor development in the mammalian inner ear

20 June 2018

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Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk

20 June 2018

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Susceptibility genes for age-related maculopathy on chromosome 10q26

20 June 2018

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Interstitial lung disease in children -- genetic background and associated phenotypes

20 June 2018

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Notch signaling, brain development, and human disease

20 June 2018

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Complement factor H polymorphism in age-related macular degeneration

20 June 2018

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Complement factor H polymorphism and age-related macular degeneration

20 June 2018

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Complement factor H variant increases the risk of age-related macular degeneration

20 June 2018

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Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation

20 June 2018

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Dissection of genomewide-scan data in extended families reveals a major locus and oligogenic susceptibility for age-related macular degeneration

20 June 2018

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Evidence of RPGRIP1 gene mutations associated with recessive cone-rod dystrophy

20 June 2018

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Analysis of gene expression in the developing mouse retina

20 June 2018

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Six3 and Six6 activity is modulated by members of the groucho family

20 June 2018

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Analysis of the Arg345Trp disease-associated allele of the EFEMP1 gene in individuals with early onset drusen or familial age-related macular degeneration

20 June 2018

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VSX1: a gene for posterior polymorphous dystrophy and keratoconus

20 June 2018

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Haploinsufficiency of NSD1 causes Sotos syndrome

20 June 2018

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Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice

20 June 2018

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Simple and complex ABCR: genetic predisposition to retinal disease

20 June 2018

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Further evidence for an association of ABCR alleles with age-related macular degeneration. The International ABCR Screening Consortium

20 June 2018

1 reference

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VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies

20 June 2018

1 reference

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Genealogies of mouse inbred strains

20 June 2018

1 reference

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A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy

20 June 2018

1 reference

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ATP binding cassette transporter retina genotypes and age related macular degeneration: an analysis on exudative non-familial Japanese patients

20 June 2018

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The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

20 June 2018

1 reference

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Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration

20 June 2018

1 reference

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Behavioral phenotypes of inbred mouse strains: implications and recommendations for molecular studies

20 June 2018

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The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoprotein.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136482

Effect of genetic background on acoustic startle response in fragile X knockout mice

20 June 2018

1 reference

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Mapping of genetic modifiers of Nr2e3 rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantity

21 January 2018

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https://api.crossref.org/works/10.1371/JOURNAL.PONE.0021858

Electroconvulsive thresholds of inbred mouse strains

21 January 2018

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Visual detection, pattern discrimination and visual acuity in 14 strains of mice

21 January 2018

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Survey of 21 inbred mouse strains in two laboratories reveals that BTBR T/ tf/tf has severely reduced hippocampal commissure and absent corpus callosum

21 January 2018

1 reference

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The transcription factor Nr2e3 functions in retinal progenitors to suppress cone cell generation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0021858

Genetic modification of retinal degeneration in tubby mice

21 January 2018

1 reference

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Mapping of genetic modifiers of Eya1 ( bor/bor ) in CAST/EiJ and BALB/cJ that suppress cochlear aplasia and associated deafness

21 January 2018

1 reference

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Loss of RB1 induces non-proliferative retinoma: increasing genomic instability correlates with progression to retinoblastoma

21 January 2018

1 reference

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Slowed recovery of rod photoresponse in mice lacking the GTPase accelerating protein RGS9-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0021858

Regulation of ganglion cell production by Notch signaling during retinal development

21 January 2018

1 reference

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The murine cone photoreceptor: a single cone type expresses both S and M opsins with retinal spatial patterning

21 January 2018

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A comparison of ERG abnormalities in XLRS and XLCSNB.

21 January 2018

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Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene

21 January 2018

1 reference

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Pathfinding and error correction by retinal axons: the role of astray/robo2.

21 January 2018

1 reference

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The stromal gene encoding the CD274 antigen as a genetic modifier controlling survival of mice with γ-radiation-induced T-cell lymphoblastic lymphomas

21 January 2018

1 reference

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Wnt signaling has different temporal roles during retinal development

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136482

The CAST/Ei strain confers significant protection against Apc(Min) intestinal polyps, independent of the resistant modifier of Min 1 (Mom1) locus.

26 November 2018

1 reference

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A mouse model for Sorsby fundus dystrophy.

26 November 2018

1 reference

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Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene

26 November 2018

1 reference

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Multiple trait measurements in 43 inbred mouse strains capture the phenotypic diversity characteristic of human populations

26 November 2018

1 reference

12 December 2020

Coding and noncoding variants in the CFH gene and cigarette smoking influence the risk of age-related macular degeneration in a Japanese population

1 reference

12 December 2020

Age-related macular degeneration

1 reference

12 December 2020

Analysis of the Stargardt disease gene (ABCR) in age-related macular degeneration

1 reference

12 December 2020

Retinitis pigmentosa associated with rhodopsin mutations: Correlation between phenotypic variability and molecular effects

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0021858

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release_3ulfb5t7cree5jfmiqnw2lqbhq

19 October 2017

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https://api.fatcat.wiki/v0/release/3ulfb5t7cree5jfmiqnw2lqbhq

24 November 2022

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19 October 2017

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